Matthew Burge

ORCID: 0000-0003-2562-7806
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About
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Research Areas
  • Colorectal Cancer Treatments and Studies
  • Genetic factors in colorectal cancer
  • Cancer Genomics and Diagnostics
  • Gastric Cancer Management and Outcomes
  • Pancreatic and Hepatic Oncology Research
  • Neuroendocrine Tumor Research Advances
  • Colorectal Cancer Surgical Treatments
  • Cancer Immunotherapy and Biomarkers
  • Cancer Treatment and Pharmacology
  • Lung Cancer Treatments and Mutations
  • Colorectal and Anal Carcinomas
  • Economic and Financial Impacts of Cancer
  • Radiopharmaceutical Chemistry and Applications
  • Lung Cancer Research Studies
  • Neuroblastoma Research and Treatments
  • Esophageal Cancer Research and Treatment
  • Hepatocellular Carcinoma Treatment and Prognosis
  • HER2/EGFR in Cancer Research
  • Renal cell carcinoma treatment
  • Multiple and Secondary Primary Cancers
  • Health Systems, Economic Evaluations, Quality of Life
  • Cancer, Lipids, and Metabolism
  • Cancer Cells and Metastasis
  • Cancer survivorship and care
  • Cancer, Hypoxia, and Metabolism

Royal Brisbane and Women's Hospital
2016-2025

The University of Queensland
2016-2024

St Bartholomew's Hospital
2024

Royal Ottawa Mental Health Centre
2023

Prince Charles Hospital
2004-2023

QIMR Berghofer Medical Research Institute
2020-2023

Prince Charles Hospital
2023

Cancer Care Services
2019

Lyell McEwin Hospital
2018

Blandford Community Hospital
2017

KEYNOTE-164 (NCT02460198) evaluated the antitumor activity of pembrolizumab in previously treated, metastatic, microsatellite instability-high/mismatch repair-deficient (MSI-H/dMMR) colorectal cancer (CRC).This phase II open-label study involved 128 centers worldwide. Eligible patients were age ≥ 18 years and had metastatic MSI-H/dMMR CRC treated with 2 prior lines standard therapy, including fluoropyrimidine, oxaliplatin, irinotecan or without anti-vascular endothelial growth...

10.1200/jco.19.02107 article EN Journal of Clinical Oncology 2019-11-14

The role of adjuvant chemotherapy in stage II colon cancer continues to be debated. presence circulating tumor DNA (ctDNA) after surgery predicts very poor recurrence-free survival, whereas its absence a low risk recurrence. benefit for ctDNA-positive patients is not well understood.

10.1056/nejmoa2200075 article EN New England Journal of Medicine 2022-06-04

Data suggest selective internal radiotherapy (SIRT) in third-line or subsequent therapy for metastatic colorectal cancer has clinical benefit patients with liver metastases liver-dominant disease after chemotherapy. The FOXFIRE, SIRFLOX, and FOXFIRE-Global randomised studies evaluated the efficacy of combining first-line chemotherapy SIRT using yttrium-90 resin microspheres metastases. were designed combined analysis overall survival.

10.1016/s1470-2045(17)30457-6 article EN cc-by The Lancet Oncology 2017-08-03

For patients with locally advanced rectal cancer (LARC), adjuvant chemotherapy selection following surgery remains a major clinical dilemma. Here, we investigated the ability of circulating tumour DNA (ctDNA) to improve risk stratification in LARC.We enrolled LARC (T3/T4 and/or N+) planned for neoadjuvant chemoradiotherapy. Plasma samples were collected pretreatment, postchemoradiotherapy and 4-10 weeks after surgery. Somatic mutations individual patient's identified via massively parallel...

10.1136/gutjnl-2017-315852 article EN Gut 2018-02-02

In patients with resectable colorectal liver metastases (CRLM), the role of pre- and postoperative systemic therapy continues to be debated. Previous studies have shown that circulating tumor DNA (ctDNA) analysis, as a marker minimal residual disease, is powerful prognostic factor in nonmetastatic cancer (CRC). Serial analysis ctDNA CRLM could inform optimal use perioperative chemotherapy. Here, we performed validation study confirm impact observed previous discovery study.We prospectively...

10.1371/journal.pmed.1003620 article EN cc-by PLoS Medicine 2021-05-03
Margaret A. Tempero Uwe Pelzer Eileen M. O’Reilly Jordan M. Winter Do‐Youn Oh and 95 more Chung‐Pin Li Giampaolo Tortora Heung-Moon Chang Charles D. Lopez Tanios Bekaii‐Saab Andrew H. Ko Armando Santoro Joon Oh Park Marcus Smith Noel Giovanni Luca Frassineti Yan‐Shen Shan Andrew Dean Hanno Riess Eric Van Cutsem Jordan Berlin Philip Philip Malcolm J. Moore David Goldstein Josep Tabernero Mingyu Li Stefano Ferrara Yvan Le Bruchec George Zhang Brian Lu Andrew V. Biankin Michele Reni Richard A. Epstein Paul L. Vasey Jeremy Shapiro Matthew Burge Yu Jo Chua Marion Harris Nick Pavlakis Niall C. Tebbutt Gerald W. Prager Christian Dittrich Alois Lang Kathrin Philipp‐Abbrederis Richard Greil Herbert Stöger Michael Girschikofsky Thomas Kuehr Jean–Luc Van Laethem Stéphanie Laurent Neesha C. Dhani Yoo Joung Ko Scot Dowden Petr Kavan Mustapha Édouard Tehfe Eugen Kubala Milan Kohoutek Per Pfeiffer Mette Yilmaz Vibeke Parner Tapio Salminen Leena‐Maija Soveri Eija Korkeila Pia Österlund Julien Taı̈eb David Tougeron Pascal Artru François‐Xavier Caroli‐Bosc Rosine Guimbaud Anthony Turpin Thomas Walter Jean‐Baptiste Bachet Volker Kunzmann Florian Kreth Andreas De Block Marino Venerito Helmut Oettle Meinolf Karthaus Jörg Trojan Gunnar Folprecht Markus M. Lerch Frank Kullmann Marcel Reiser Volker Heinemann Marcus‐Alexander Wörns H. Schulz Benjamin Garlipp Thomas Yau Lam Stephen Chan Balázs Juhász László Landherr Tamàs Pintér G. Bodoky Zsuzsanna Kahán Ray McDermott Derek G. Power Luca Gianni Salvatore Siena Michèle Milella Alfredo Falcone Rossana Berardi

This randomized, open-label trial compared the efficacy and safety of adjuvant

10.1200/jco.22.01134 article EN cc-by-nc-nd Journal of Clinical Oncology 2022-12-15
Akihito Kawazoe Rui‐Hua Xu Pilar García‐Alfonso Maria Passhak Hao‐Wei Teng and 95 more Ardaman Shergill Mahmut Gümüş Camilla Qvortrup Sebastian Stintzing Kathryn Towns Tae Won Kim Kai‐Keen Shiu Juan Cundom Sumitra Ananda A. A. Lebedinets Rong Fu Rishi Jain David E. Adelberg Volker Heinemann Takayuki Yoshino Elena Élez Juan Cundom Ezequiel Slutsky Julieta Grasselli Luis Fein Luciana Bella Quero Warren Joubert Peter Gibbs Timothy Price Matthew Burge Sumitra Ananda Muhammad A. Khattak Bruce Colwell Félix Couture Brandon M. Meyers Kathryn Towns Michael B. Sawyer Lucas Sidéris Rui‐Hua Xu Wei Wang Hongming Pan Per Pfeiffer Lars Henrik Jensen Camilla Qvortrup Sebastian Stintzing Dirk Arnold Sylvie Lorenzen Stefan Kubicka Reinhard Depenbusch Maria Passhak Ravit Geva Ayala Hubert Einat Shacham‐Shmueli Gleb Kornev Akihito Kawazoe Toshiki Masuishi Atsuo Takashima Hiroki Hara Hisato Kawakami Nozomu Machida Kentaro Yamazaki Hisateru Yasui Akihito Tsuji Taito Esaki Kensei Yamaguchi Tae‐You Kim Joong Bae Ahn Myung Ah Lee Tae Won Kim Joon Oh Park Soo Hyun Lee Р. В. Орлова Vladislav O. Sarzhevskiy Marina Sekacheva S. Tjulandin Oksana Shirokova A.I. Iskhakova Iskhakova A. A. Lebedinets Paula Jiménez Fonseca F. Rivera Herrero Elena Élez Pilar Alfonso M.J. Gómez Reina Kun‐Huei Yeh Hao‐Wei Teng Tsai Sheng Yang Hwei‐Ming Wang Yu‐Min Yeh Mustafa Özgüroğlu Mahmut Gümüş Şuayib Yalçın Bülent Erdoğan Umut Demırcı Pınar Gürsoy Hakan Harputluoğlu Atakan Demir Kai‐Keen Shiu Ewan Brown Paul J. Ross Elizabeth Smyth

Treatment options are limited for patients with previously treated metastatic colorectal cancer (mCRC). In the LEAP-017 study, we evaluate whether lenvatinib in combination pembrolizumab improves outcomes compared standard of care (SOC) mismatch repair proficient or not microsatellite instability high (pMMR MSI-H) mCRC.

10.1200/jco.23.02736 article EN cc-by-nc-nd Journal of Clinical Oncology 2024-06-04

Open-label phase II study (RELATIVITY-060) to investigate the efficacy and safety of first-line nivolumab, a PD-1-blocking antibody, plus relatlimab, lymphocyte-activation gene 3 (LAG-3)-blocking chemotherapy in patients with previously untreated advanced gastric cancer (GC) or gastroesophageal junction (GEJC).

10.1200/jco.23.01636 article EN Journal of Clinical Oncology 2024-05-09

// Catherine E. Bond 1 , Diane M. McKeone Murugan Kalimutho 2 Mark L. Bettington 1, 3, 4 Sally-Ann Pearson Troy D. Dumenil Leesa F. Wockner 5 Matthew Burge 6 Barbara A. Leggett 4, 7 Vicki L.J. Whitehall 8 Conjoint Gastroenterology Laboratory, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia Signal Transduction 3 Envoi Specialist Pathologists, School of Medicine, University Cancer and Population Studies, Department Oncology, Royal Brisbane Women's Hospital,...

10.18632/oncotarget.12130 article EN Oncotarget 2016-09-20

Abstract Background: There is strong interest in testing lifestyle interventions to improve cancer outcomes; however, the optimal methods for achieving behavior change large-scale pragmatic trials are unknown. Here, we report 1-year feasibility results exercise Canadian Cancer Trials Group CO.21 (CHALLENGE) Trial. Methods: Between 2009 and 2014, 273 high-risk stage II III colon survivors from 42 centers Canada Australia were randomized a structured program (SEP; n = 136) or health education...

10.1158/1055-9965.epi-15-1267 article EN Cancer Epidemiology Biomarkers & Prevention 2016-04-09

Abstract Studies in multiple solid tumor types have demonstrated the prognostic significance of ctDNA analysis after curative intent surgery. A combined data across completed studies could further our understanding circulating DNA (ctDNA) as a marker and inform future trial design. We individual patient from three independent cohort nonmetastatic colorectal cancer (CRC). Plasma samples were collected 4 to 10 weeks Mutations assayed using massively parallel sequencing technique called...

10.1002/ijc.33312 article EN International Journal of Cancer 2020-09-28

107 Background: Recurrence rates following upfront resection of pancreatic adenocarcinoma are high, with some benefit from adjuvant chemotherapy (AC). A biomarker that improves risk stratification and/or provides real time indication AC could improve routine clinical management and accelerate trial progress. Previous studies in pancreas cancer suggest patients detectable ctDNA post surgery at an elevated recurrence. Detectable the completion may also be associated recurrence risk. Methods:...

10.1200/jco.2024.42.16_suppl.107 article EN Journal of Clinical Oncology 2024-06-01

3514 Background: Pembrolizumab is approved for the treatment of adult and pediatric patients (pts) with previously treated MSI-H cancer regardless tumor type or site. This approval was based in part on data from cohort A phase 2 KEYNOTE-164 (NCT02460198) study pts CRC after ≥2 prior lines therapy including fluoropyrimidine, oxaliplatin, irinotecan. In addition, Cohort B KEYNOTE-164, we evaluated activity pembrolizumab metastatic ≥1 line therapy. Methods: enrolled CRC, status confirmed...

10.1200/jco.2018.36.15_suppl.3514 article EN Journal of Clinical Oncology 2018-05-20
Peter Gibbs Volker Heinemann Navesh Sharma Julien Taı̈eb Jens Ricke and 95 more Marc Peeters Michael Findlay Bridget A. Robinson Christopher Jackson Andrew Strickland Val Gebski Mark Van Buskirk Huaqing Zhao Guy van Hazel Michael D. Brown Matthew Burge Giuseppe Cardaci Stephen Clarke Paul Eliadis Tom Ferguson Vinod Ganju Peter Gibbs Guy van Hazel Philip E. James Christos S. Karapetis Winston Liauw Gavin Marx Marco Matos Louise Nott Nick Pavlakis Alex Powell Timothy Price David Ransom Eva Segelov Jenny Shannon Nimit Singhal Andrew Strickland Euan Walpole Michel Craninx Thierry Delaunoit Amélie Deleporte Michel Ferrante Karen Geboes Alain Hendlisz Koen Hendrickx Marc De Man Els Monsaert Veerle Moons Marc Peeters Marc Polus Éveline Boucher Jacques Balosso P. Chevallier Samy Louafi Marc Pracht Christine Rebischung Denis Smith Julien Taı̈eb Eric Terrebonne Harald-Robert Bruch Gerald Gehbauer Volker Heinemann Thomas Helmberger Yon-Dschun Ko H. Kröning Frank Lammert Arnd Nusch Stefan Pluntke Karsten Ridwelski Jorge Riera‐Knorrenschild Hanno Riess Jorge Ramon Riera Jens Ricke Tilmann Sauerbruch Klemens Scheidhauer Oliver Stötzer Klaus Tatsch Ursula Vehling‐Kaiser Thomas Vogl Alex Beny Ravit Geva Einat Shacham‐Shmueli Salomon M. Stemmer Thomas Tichler Ido Wolf Bruna Angelelli Andrea Martoni Michael Findlay Richard Isaacs Anne O’Donnell‐Luria D Díaz Pérez Bridget A. Robinson Javier Rodríguez Ruth Vera Pradip Amin Daniel Bloomgarden James T. Bui James Carlisle Seungjean Chai Yi‐Jen Chen

10.1016/j.clcc.2018.06.001 article EN Clinical Colorectal Cancer 2018-06-13

AimWe evaluated pembrolizumab monotherapy in patients with advanced salivary gland carcinoma on the phase 2 KEYNOTE-158 study (NCT02628067).MethodsEligible had histologically/cytologically confirmed prior failure or intolerance to standard therapy, measurable disease per Response Evaluation Criteria Solid Tumours (RECIST) v1.1., and ECOG performance status 0–1. Patients were enrolled irrespective of tumour PD-L1 expression. received 200 mg Q3W for up 35 cycles (∼2 years). Radiographic...

10.1016/j.ejca.2022.05.007 article EN cc-by-nc-nd European Journal of Cancer 2022-06-28

Background Pixatimod is a unique activator of the Toll-like Receptor 9 pathway. This phase I trial evaluated safety, efficacy and pharmacodynamics pixatimod PD-1 inhibitor nivolumab in immunologically cold cancers. Methods 3+3 dose escalation with microsatellite stable metastatic colorectal cancer (MSS mCRC) pancreatic ductal adenocarcinoma (mPDAC) expansion cohorts. Participants received once weekly as 1-hour intravenous infusion plus every 2 weeks. Objectives included assessment antitumor...

10.1136/jitc-2022-006136 article EN cc-by-nc Journal for ImmunoTherapy of Cancer 2023-01-01

108 Background: Previous results of the DYNAMIC study demonstrated that a ctDNA-guided approach versus standard management in stage II colon cancer (CC) reduced adjuvant chemotherapy (ACT) use without compromising 2-year recurrence-free survival (RFS). MMR status defines two distinct subsets CC. Here, we report impact ctDNA burden, end ACT (EOT) ctDNA, and updated data including overall (OS). Methods: is multi-center randomized phase trial. Eligible patients (pts) had resected CC were...

10.1200/jco.2024.42.16_suppl.108 article EN Journal of Clinical Oncology 2024-05-29

Abstract Purpose: Duligotuzumab is a dual-action antibody directed against EGFR and HER3. Experimental Design: Metastatic colorectal cancer (mCRC) patients with KRAS ex2 wild-type received duligotuzumab or cetuximab FOLFIRI until progression intolerable toxicity. Mandatory tumor samples underwent mutation biomarker analysis. Efficacy analysis was conducted in RAS exon 2/3 tumors. Results: Of 134 randomly assigned patients, 98 had ex2/3 wild-type. provided no progression-free survival (PFS)...

10.1158/1078-0432.ccr-17-0646 article EN Clinical Cancer Research 2018-03-05

Highlights•EMR 5-year survival >50%.•Docetaxel + CF improves histological responses for MNR.•DCF RT MNR.AbstractBackgroundPatients with oesophageal/gastro-oesophageal junction adenocarcinoma (EAC) not showing early metabolic response (EMR) to chemotherapy have poorer and rates <5%. We investigated whether tailoring neoadjuvant therapy can improve outcomes in these patients.Patients methodsPatients resectable EAC were enrolled randomised into two single-arm, multicentre phase II trials. After...

10.1016/j.annonc.2019.10.019 article EN publisher-specific-oa Annals of Oncology 2020-01-06
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